ArticleNature communications2026
Lipopolysaccharide insertion and vesicle mediated turnover drive growth independent outer membrane adaptation in Escherichia coli.
Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Lipopolysaccharide insertion and vesicle mediated turnover drive growth independent outer membrane adaptation in Escherichia coli.Nature communications · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
The Gram-negative outer membrane is a load-bearing permeability barrier dependent on ordered lipopolysaccharide (LPS) packing in its outer leaflet. How this organisation is maintained after LPS insertion, and whether bacteria can remodel LPS independently of growth, remain unclear. Existing models attribute LPS turnover to passive dilution during elongation and division, limiting adaptation as growth slows. Here we show that, as Escherichia coli enters stationary phase and elongation slows, new LPS insertion continues while pre-existing LPS is preferentially removed through outer membrane vesicles, enabling growth-independent surface remodelling. Pulse-chase metabolic labelling and super-resolution microscopy reveal that newly inserted LPS localises to discrete sites and remains segregated from pre-existing LPS. Spatiotemporal analysis supports an insertion-trapping model in which localised insertion and restricted lateral diffusion maintain LPS-rich patches without coarsening into larger domains. Time-lapse imaging, biochemical fractionation and nanoparticle tracking identify vesicle release as a route that uncouples LPS turnover from cell growth.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.